Electrocatalytic Minisci Acylation Reaction of N-Heteroarenes Mediated by NH4I-Reference-Cited by-同舟云学术

Electrocatalytic Minisci Acylation Reaction of N-Heteroarenes Mediated by NH4I

Published:2017-10-02 Issue:20 Volume:19 Page:5517-5520
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Qing-Qing¹,Xu Kun¹²,Jiang Yang-Ye¹,Liu Yong-Guo³,Sun Bao-Guo³,Zeng Cheng-Chu¹^ORCID

Affiliation:

1. Beijing Key Laboratory of Environmental and Viral Oncology, College of Life Science & Bioengineering, Beijing University of Technology, Beijing 100124, China

2. College of Chemistry and Pharmaceutical Engineering, Nanyang Normal University, Nanyang, Henan 473061, China

3. Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, Beijing 100048, China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b02589

Reference45 articles.

1. Minisci reactions: Versatile CH-functionalizations for medicinal chemists

2. Radical Addition to Iminium Ions and Cationic Heterocycles

3. Direct alkylation of heteroarenes with unactivated bromoalkanes using photoredox gold catalysis

4. A visible-light-promoted radical reaction system for azidation and halogenation of tertiary aliphatic C–H bonds

5. Photoredox-mediated Minisci C–H alkylation of N-heteroarenes using boronic acids and hypervalent iodine

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